Technology Process of (2S,3S,4S,5R,6S)-3-((2R,3R,4R,5S,6R)-4,5-Diacetoxy-6-acetoxymethyl-3-azido-tetrahydro-pyran-2-yloxy)-6-hydroxy-4,5-bis-(4-methyl-benzoyloxy)-tetrahydro-pyran-2-carboxylic acid methyl ester
There total 10 articles about (2S,3S,4S,5R,6S)-3-((2R,3R,4R,5S,6R)-4,5-Diacetoxy-6-acetoxymethyl-3-azido-tetrahydro-pyran-2-yloxy)-6-hydroxy-4,5-bis-(4-methyl-benzoyloxy)-tetrahydro-pyran-2-carboxylic acid methyl ester which
guide to synthetic route it.
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synthetic route:
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180274-58-2
(2S,3S,4S,5R,6S)-3-((2R,3R,4R,5S,6R)-4,5-Diacetoxy-6-acetoxymethyl-3-azido-tetrahydro-pyran-2-yloxy)-6-(4-methoxy-phenoxy)-4,5-bis-(4-methyl-benzoyloxy)-tetrahydro-pyran-2-carboxylic acid methyl ester
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180274-59-3
(2S,3S,4S,5R,6S)-3-((2R,3R,4R,5S,6R)-4,5-Diacetoxy-6-acetoxymethyl-3-azido-tetrahydro-pyran-2-yloxy)-6-hydroxy-4,5-bis-(4-methyl-benzoyloxy)-tetrahydro-pyran-2-carboxylic acid methyl ester
- Guidance literature:
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With
ammonium cerium(IV) nitrate;
In
acetonitrile;
at 0 ℃;
for 2h;
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180274-59-3
(2S,3S,4S,5R,6S)-3-((2R,3R,4R,5S,6R)-4,5-Diacetoxy-6-acetoxymethyl-3-azido-tetrahydro-pyran-2-yloxy)-6-hydroxy-4,5-bis-(4-methyl-benzoyloxy)-tetrahydro-pyran-2-carboxylic acid methyl ester
- Guidance literature:
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Multi-step reaction with 10 steps
1: 73 percent / p-TSA / 1 h / Ambient temperature
2: pyridine
3: MeOH, camphorsulfonic acid / Ambient temperature
4: 99 percent / imidazole / dimethylformamide
5: 42 percent / AgOTf, molecular sieves 4 Angstroem / CH2Cl2 / 1.) r.t., 40 min, 2.) 0 deg C, 1.5 h; r.t., 1 day
6: 89 percent / TBAF, AcOH / tetrahydrofuran / 120 h / Ambient temperature
7: 1.) DMSO, (COCl)2, 2.) DIPEA / 1.) CH2Cl2, -78 deg C, 30 min, 2.) 35 min
8: aq. NaClO2, NaH2PO4, 2-methyl-2-butene / 2-methyl-propan-2-ol
9: ethyl acetate; diethyl ether
10: 88 percent / aq. CAN / acetonitrile / 2 h / 0 °C
With
pyridine; 1H-imidazole; methanol; sodium chlorite; sodium dihydrogenphosphate; 2-methyl-but-2-ene; oxalyl dichloride; ammonium cerium(IV) nitrate; 4 A molecular sieve; camphor-10-sulfonic acid; tetrabutyl ammonium fluoride; silver trifluoromethanesulfonate; acetic acid; dimethyl sulfoxide; N-ethyl-N,N-diisopropylamine;
toluene-4-sulfonic acid;
In
tetrahydrofuran; diethyl ether; dichloromethane; ethyl acetate; N,N-dimethyl-formamide; acetonitrile; tert-butyl alcohol;
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180274-59-3
(2S,3S,4S,5R,6S)-3-((2R,3R,4R,5S,6R)-4,5-Diacetoxy-6-acetoxymethyl-3-azido-tetrahydro-pyran-2-yloxy)-6-hydroxy-4,5-bis-(4-methyl-benzoyloxy)-tetrahydro-pyran-2-carboxylic acid methyl ester
- Guidance literature:
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Multi-step reaction with 6 steps
1: 42 percent / AgOTf, molecular sieves 4 Angstroem / CH2Cl2 / 1.) r.t., 40 min, 2.) 0 deg C, 1.5 h; r.t., 1 day
2: 89 percent / TBAF, AcOH / tetrahydrofuran / 120 h / Ambient temperature
3: 1.) DMSO, (COCl)2, 2.) DIPEA / 1.) CH2Cl2, -78 deg C, 30 min, 2.) 35 min
4: aq. NaClO2, NaH2PO4, 2-methyl-2-butene / 2-methyl-propan-2-ol
5: ethyl acetate; diethyl ether
6: 88 percent / aq. CAN / acetonitrile / 2 h / 0 °C
With
sodium chlorite; sodium dihydrogenphosphate; 2-methyl-but-2-ene; oxalyl dichloride; ammonium cerium(IV) nitrate; 4 A molecular sieve; tetrabutyl ammonium fluoride; silver trifluoromethanesulfonate; acetic acid; dimethyl sulfoxide; N-ethyl-N,N-diisopropylamine;
In
tetrahydrofuran; diethyl ether; dichloromethane; ethyl acetate; acetonitrile; tert-butyl alcohol;